Welcome to the new version of CaltechAUTHORS. Login is currently restricted to library staff. If you notice any issues, please email coda@library.caltech.edu
Published February 3, 2009 | Accepted Version
Journal Article Open

Common Mitochondrial DNA Mutations Generated through DNA-Mediated Charge Transport


Mutation sites that arise in human mitochondrial DNA as a result of oxidation by a rhodium photooxidant have been identified. HeLa cells were incubated with [Rh(phi)2bpy]Cl3 (phi is 9,10-phenanthrenequinone diimine), an intercalating photooxidant, to allow the complex to enter the cell and bind mitochondrial DNA. Photoexcitation of DNA-bound [Rh(phi)2bpy]3+ can promote the oxidation of guanine from a distance through DNA-mediated charge transport. After two rounds of photolysis and growth of cells incubated with the rhodium complex, DNA mutations in a portion of the mitochondrial genome were assessed via manual sequencing. The mutational pattern is consistent with dG to dT transversions in the repetitive guanine tracts. Significantly, the mutational pattern found overlaps oxidative damage hot spots seen previously. These mutations are found within conserved sequence block II, a critical regulatory element involved in DNA replication, and these have been identified as sites of low oxidation potential to which oxidative damage is funneled. On the basis of this mutational analysis and its correspondence to sites of long-range oxidative damage, we infer a critical role for DNA charge transport in generating these mutations and, thus, in regulating mitochondrial DNA replication under oxidative stress.

Additional Information

© 2009 American Chemical Society. Received August 20, 2008; Revised Manuscript Received October 31, 2008. We are grateful to the NIH (GM49216) for their financial support of this research, including a minority postdoctoral fellowship to E.J.M.

Attached Files

Accepted Version - nihms91341.pdf


Files (1.8 MB)
Name Size Download all
1.8 MB Preview Download

Additional details

August 20, 2023
October 19, 2023